Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Astn1 |
T |
C |
1: 158,407,897 (GRCm39) |
I618T |
possibly damaging |
Het |
Bod1l |
T |
C |
5: 41,989,593 (GRCm39) |
S377G |
probably benign |
Het |
Disp2 |
A |
T |
2: 118,621,361 (GRCm39) |
S698C |
probably damaging |
Het |
Ehbp1l1 |
A |
G |
19: 5,773,012 (GRCm39) |
V43A |
probably damaging |
Het |
Eml5 |
G |
T |
12: 98,765,191 (GRCm39) |
T1539K |
probably damaging |
Het |
Fmnl2 |
T |
C |
2: 53,008,380 (GRCm39) |
I824T |
probably damaging |
Het |
Gpr75 |
T |
G |
11: 30,841,132 (GRCm39) |
N12K |
probably damaging |
Het |
Hap1 |
C |
T |
11: 100,242,732 (GRCm39) |
|
probably null |
Het |
Helz2 |
A |
C |
2: 180,880,274 (GRCm39) |
Y481D |
probably benign |
Het |
Klhl3 |
T |
C |
13: 58,157,236 (GRCm39) |
|
probably null |
Het |
Lrcol1 |
A |
G |
5: 110,502,073 (GRCm39) |
S49G |
probably damaging |
Het |
Magi3 |
A |
G |
3: 103,992,560 (GRCm39) |
M304T |
probably damaging |
Het |
Med13l |
T |
C |
5: 118,731,587 (GRCm39) |
W88R |
probably damaging |
Het |
Nfatc1 |
A |
G |
18: 80,710,257 (GRCm39) |
V503A |
probably damaging |
Het |
Ntm |
C |
A |
9: 29,322,886 (GRCm39) |
V45L |
probably benign |
Het |
Or4c100 |
A |
G |
2: 88,356,767 (GRCm39) |
N280S |
probably damaging |
Het |
Or4f60 |
T |
A |
2: 111,902,266 (GRCm39) |
I221L |
probably benign |
Het |
Or4p22 |
T |
A |
2: 88,317,270 (GRCm39) |
S65T |
possibly damaging |
Het |
Or5b116 |
A |
G |
19: 13,422,526 (GRCm39) |
D50G |
probably damaging |
Het |
Or7a40 |
T |
C |
16: 16,490,967 (GRCm39) |
R293G |
probably damaging |
Het |
Pias4 |
T |
C |
10: 80,993,332 (GRCm39) |
Q197R |
probably damaging |
Het |
Pkhd1 |
T |
A |
1: 20,628,895 (GRCm39) |
H684L |
probably damaging |
Het |
Prr5 |
A |
C |
15: 84,651,415 (GRCm39) |
I288L |
possibly damaging |
Het |
Psmb3 |
T |
A |
11: 97,603,336 (GRCm39) |
M183K |
probably damaging |
Het |
Rasal1 |
T |
C |
5: 120,808,383 (GRCm39) |
F472L |
possibly damaging |
Het |
Rpl3 |
A |
T |
15: 79,964,061 (GRCm39) |
|
probably benign |
Het |
Scin |
A |
T |
12: 40,113,256 (GRCm39) |
D538E |
probably benign |
Het |
Sdhb |
T |
C |
4: 140,701,038 (GRCm39) |
S165P |
probably benign |
Het |
Slc43a2 |
C |
A |
11: 75,436,577 (GRCm39) |
|
probably null |
Het |
Sparc |
C |
T |
11: 55,298,041 (GRCm39) |
|
probably null |
Het |
Tcf25 |
A |
G |
8: 124,119,975 (GRCm39) |
E382G |
possibly damaging |
Het |
Tmx3 |
G |
A |
18: 90,529,458 (GRCm39) |
|
probably null |
Het |
Trim24 |
C |
T |
6: 37,922,548 (GRCm39) |
P452S |
probably benign |
Het |
Vsig10 |
T |
A |
5: 117,476,379 (GRCm39) |
W278R |
probably damaging |
Het |
|
Other mutations in Speer4c2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Speer4c2
|
APN |
5 |
15,861,884 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL00088:Speer4c2
|
APN |
5 |
15,861,884 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL01443:Speer4c2
|
APN |
5 |
15,857,642 (GRCm39) |
makesense |
probably null |
|
IGL01789:Speer4c2
|
APN |
5 |
15,861,884 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL01791:Speer4c2
|
APN |
5 |
15,861,884 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL01792:Speer4c2
|
APN |
5 |
15,861,884 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL01795:Speer4c2
|
APN |
5 |
15,861,884 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02344:Speer4c2
|
APN |
5 |
15,861,884 (GRCm39) |
utr 5 prime |
probably benign |
|
R8385:Speer4c2
|
UTSW |
5 |
15,857,669 (GRCm39) |
missense |
unknown |
|
R8990:Speer4c2
|
UTSW |
5 |
15,858,598 (GRCm39) |
missense |
probably benign |
|
|